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Objective Our objective was to determine effects of supplemental fat sources on digestion and energy predictions in feedlot diets containing several lipid sources. Materials and Methods Five ruminally fistulated steers (520 ± 41 kg of BW) were fed in a 5-period Latin square design. Dietary treatments included control (CORN) or 4 finishing diets containing (1) 4.8% added corn oil (OIL), (2) 4.8% beef tallow (TAL), (3) 25.5% corn condensed distillers solubles (CCDS), or (4) 56% wet distillers grains plus solubles (WDGS). Total-tract OM digestibility was multiplied by dietary OM content to determine digested OM (DIGOM; % of DM). Measured dietary DE (Mcal/kg) was converted to TDN using 4.4 Mcal of DE/kg of TDN. Results and Discussion The unsaturated-to-saturated total fatty acid ratio of omasal samples of steers fed WDGS was greater than that for other treatments (P = 0.01). Apparent total-tract diet NDF digestibility was least for steers fed OIL (P Implications and Applications In finishing diets containing WDGS, additional DE is not accounted for when evaluating only DIGOM. Measuring DE content of diets used in digestion trials is important when trying to estimate feeding values.

Three experiments evaluated the effects of corn oil removal using centrifugation in ethanol plants, on animal performance and digestion characteristics by finishing cattle fed by-products. In Exp. 1, 225 crossbred steers (300 ± 9.1 kg) were utilized in a randomized block design with a 2 × 2 + 1 factorial arrangement of treatments. Factors consisted of oil concentration [de-oiled (DO) or full fat (FF)] and by-product type [condensed distillers solubles (CDS) or modified distillers grains plus solubles (MDGS)] compared to a corn-based control. Fat concentration was 6.0% for DO CDS, 21.1% for FF CDS, 9.2% for DO MDGS, and 11.8% for FF MDGS. No oil concentration by by-product type interactions (P ≥ 0.17) were observed. There were no differences in DMI, ADG, or G:F between DO and FF CDS (P ≥ 0.29) or DO and FF MDGS (P ≥ 0.58). No differences (P ≥ 0.25) due to oil concentration were observed for carcass characteristics. Experiment 2 was a 5 × 5 Latin Square digestion trial with treatments similar to Exp. 1. Fat concentration was 8.7% or 15.4% for DO or FF CDS and 9.2% or 12.3% for DO or FF MDGS. Intake and total tract digestibility of fat were greater (P ≤ 0.02) for FF CDS compared with DO CDS. Digestible energy (megacalorie per kilogram), adjusted for intake, was greater (P = 0.02) for steers fed FF CDS compared to DO CDS. Average ruminal pH for cattle fed FF MDGS was greater than DO MDGS (P = 0.06). In Exp. 3, 336 yearling, crossbred steers (352 ± 19 kg) were utilized in a randomized block design with a 2 × 3 + 1 factorial arrangement of treatments. Factors included oil concentration (DO or FF) and inclusion [35%, 50%, and 65% wet distillers grains plus solubles (WDGS)] along with a corn-based control. The fat concentrations of DO and FF WDGS were 7.9% and 12.4%, respectively. A linear interaction (P < 0.01) was observed for DMI, which produced different slopes for DO and FF WDGS. No linear or quadratic interactions were observed for BW, ADG, or G:F (P ≥ 0.31). For the main effect of oil concentration, there were no statistical differences (P > 0.19) for final BW, ADG, or G:F. No statistical differences were observed for all carcass traits (P ≥ 0.34). Corn oil removal via centrifugation had minimal impact on finishing performance suggesting that cattle fed DO by-products will have similar performance to cattle fed FF by-products in dry-rolled and high-moisture corn diets.

Two experiments evaluated the effects of corn residue harvest method on animal performance and diet digestibility. Experiment 1 was designed as a 2 × 2 + 1 factorial arrangement of treatments using 60 individually fed crossbred steers (280 kg [SD 32] initial BW; n = 12). Factors were the corn residue harvest method (high-stem and conventional) and supplemental RUP at 2 concentrations (0 and 3.3% diet DM). A third harvest method (low-stem) was also evaluated, but only in diets containing supplemental RUP at 3.3% diet DM because of limitations in the amount of available low-stem residue. Therefore, the 3 harvest methods were compared only in diets containing supplemental RUP. In Exp. 2, 9 crossbred wethers were blocked by BW (42.4 kg [SD 7] initial BW) and randomly assigned to diets containing corn residue harvested 1 of 3 ways (low-stem, high-stem, and conventional). In Exp. 1, steers fed the low-stem residue diet had greater ADG compared with the steers fed conventionally harvested corn residue (P = 0.03; 0.78 vs. 0.63 kg), whereas steers fed high-stem residue were intermediate (P > 0.17; 0.69 kg), not differing from either conventional or low-stem residues. Results from in vitro OM digestibility suggest that low-stem residue had the greatest (P < 0.01) amount of digestible OM compared with the other 2 residue harvest methods, which did not differ (P = 0.32; 55.0, 47.8, and 47.1% for low-stem, high-stem, and conventional residues, respectively). There were no differences in RUP content (40% of CP) and RUP digestibility (60%) among the 3 residues (P ≥ 0.35). No interactions were observed between harvest method and the addition of RUP (P ≥ 0.12). The addition of RUP tended to result in improved ADG (0.66 ± 0.07 vs. 0.58 ± 0.07 for supplemental RUP and no RUP, respectively; P = 0.08) and G:F (0.116 ± 0.006 vs. 0.095 ± 0.020 for supplemental RUP and no RUP, respectively; P = 0.02) compared with similar diets without the additional RUP. In Exp. 2, low-stem residue had greater DM and OM digestibility and DE (P < 0.01) than high-stem and conventional residues, which did not differ (P ≥ 0.63). Low-stem residue also had the greatest NDF digestibility (NDFD; P < 0.01), whereas high-stem residue had greater NDFD than conventional residue (P < 0.01). Digestible energy was greatest for low-stem residue (P < 0.05) and did not differ between high-stem and conventional residues (P = 0.50). Reducing the proportion of stem in the bale through changes in the harvest method increased the nutritive quality of corn residue.

Data from 16 trials were compiled to calculate microbial CP (MCP) production and MP requirements of growing cattle on high-forage diets. All cattle were individually fed diets with 28% to 72% corn cobs in addition to either alfalfa, corn silage, or sorghum silage at 18% to 60% of the diet (DM basis). The remainder of the diet consisted of protein supplement. Source of protein within the supplement varied and included urea, blood meal, corn gluten meal, dry distillers grains, feather meal, meat and bone meal, poultry by-product meal, soybean meal, and wet distillers grains. All trials included a urea-only treatment. Intake of all cattle within an experiment was held constant, as a percentage of BW, established by the urea-supplemented group. In each trial the base diet (forage and urea supplement) was MP deficient. Treatments consisted of increasing amounts of test protein replacing the urea supplement. As protein in the diet increased, ADG plateaued. Among experiments, ADG ranged from 0.11 to 0.73 kg. Three methods of calculating microbial efficiency were used to determine MP supply. Gain was then regressed against calculated MP supply to determine MP requirement for maintenance and gain. Method 1 (based on a constant 13% microbial efficiency as used by the beef NRC model) predicted an MP maintenance requirement of 3.8 g/kg BW and 385 g MP/kg gain. Method 2 calculated microbial efficiency using low-quality forage diets and predicted MP requirements of 3.2 g/kg BW for maintenance and 448 g/kg for gain. Method 3 (based on an equation predicting MCP yield from TDN intake, proposed by the Beef Cattle Nutrient Requirements Model [BCNRM]) predicted MP requirements of 3.1 g/kg BW for maintenance and 342 g/kg for gain. The factorial method of calculating MP maintenance requirements accounts for scurf, endogenous urinary, and metabolic fecal protein losses and averaged 4.2 g/kg BW. Cattle performance data demonstrate formulating diets to meet the beef NRC model recommended MP maintenance requirement (3.8 g/kg S) works well when using 13% microbial efficiency. Therefore, a change in how microbial efficiency is calculated necessitates a change in the proposed MP maintenance requirement to not oversupply or undersupply RUP. Using the 2016 BCNRM to predict MCP production and formulate diets to meet MP requirements also requires changing the MP maintenance requirement to 3.1 g/kg BW.

A data set of individual observations was compiled from digestibility trials to examine the relationship between the duodenal purine bases (PB) flow and urinary purine derivatives (PD) excretion and the validity of different equations for estimating rumen microbial N (Nm) supply based on urinary PD in comparison with estimates based on duodenal PB. Trials (8 trials, = 185) were conducted with male sheep fitted with a duodenal T-type cannula, housed in metabolic cages, and fed forage alone or with supplements. The amount of PD excreted in urine was linearly related to the amount of PB flowing to the duodenum (0.05). The intercept of the linear regression was 0.180 mmol/(d·kg), representing the endogenous excretion of PD, and the slope was lower than 1 (0.05), indicating that only 0.43% of the PB in the duodenum was excreted as PD in urine. The Nm supply estimated by either approach was linearly related (0.05) to the digestible OM intake. However, the Nm supply estimated through either of 3 published PD-based equations probably underestimated the Nm supply in sheep.

Two experiments were conducted to evaluate the effects of ractopamine hydrochloride (RAC) dose and duration on growth performance and carcass characteristics of finishing steers. In Exp. 1, 336 crossbred steers (initial BW of RAC feeding = 539 kg [SD 22]) were used in a 2 × 2 factorial arrangement of treatments with one factor being RAC dose (0 or 200 mg/steer daily) and the other factor being RAC duration (28 or 42 d prior to harvest). There were no RAC dose × duration interactions ( ≥ 0.08) for growth performance or carcass characteristics. Feeding 200 mg RAC/steer daily increased (0.01) live final BW by 9.0 kg compared with steers not fed RAC. Carcass-adjusted final BW, ADG, and G:F were greater (0.01) for steers fed 200 mg RAC/d compared with steers not fed RAC. Hot carcass weight was 4.7 kg heavier (0.01) for steers fed 200 mg RAC/d compared with steers not fed RAC. In Exp. 2, crossbred steers ( = 576; experiment initial BW = 408 kg [SD 29]) were used in a randomized block design with a 3 × 3 factorial arrangement of treatments. Factors included RAC dose (0, 300, and 400 mg/steer daily) and RAC duration (14, 28, or 42 d prior to harvest). There was a tendency ( ≤ 0.08) for an interaction of RAC dose × duration for final live BW, DMI, and live G:F; therefore, simple effects are presented. At 28 d, live final BW for steers fed 400 mg RAC/d were heavier (0.01) than for steers fed 0 mg RAC/d. There was a tendency at 28 d for increased live final BW for steers fed RAC at 300 mg/d ( = 0.08) compared with steers fed RAC at 0 mg and for steers fed 400 mg RAC/d compared with steers fed 300 mg RAC/d ( = 0.06). Live final BW was greater (0.01) for steers fed RAC for 42 d at 300 and 400 mg/d compared with steers fed 0 mg; however, live final BW was similar ( = 0.48) between steers fed 300 and 400 mg RAC/d. Despite no RAC dose × duration interaction ( = 0.30) for HCW, simple effects will be presented for consistency. Hot carcass weight was greater for steers fed 300 and 400 mg RAC/d for 28 and 42 d compared with steers fed 0 mg at 28 ( ≤ 0.02) and 42 d (0.01). Feeding 300 mg RAC/d for 28 or 42 d increased HCW by 5.1 and 7.6 kg, respectively, compared with steers fed 0 mg RAC. Additionally, feeding 400 mg RAC/d for 28 or 42 d resulted in increases of 8.9 and 9.4 kg, respectively, in HCW compared with steers fed 0 mg RAC. In conclusion, our results confirm that feeding RAC improves growth performance and carcass weight, with an optimal duration of feeding RAC being 28 d.

Two trials evaluated adapting cattle to a finishing diet using wet corn gluten feed compared with traditional methods using forage. A 33-d grain adaptation metabolism trial (Exp. 1) compared decreasing wet corn gluten feed (Sweet Bran; Corn Milling unit, Cargill Corn Milling, Blair, NE) while increasing corn inclusion (SB) and a traditional grain adaptation system decreasing alfalfa hay while increasing corn with no Sweet Bran inclusion (CON). Ruminal pH, intake characteristics, and 24-h in situ digestibility were evaluated using 8 ruminally fistulated steers (291 kg BW [SD 19]). Steers (4/treatment) were adapted to finishing diets across 4 periods consisting of 5, 7, 7, and 7 d and then fed a finishing diet for 7 d. No period × adaptation diet interactions were observed ( ≥ 0.12). Average ruminal pH decreased (0.01) whereas time and area below a pH of 5.6 increased ( ≤ 0.02) for the SB adaptation system compared with the CON adaptation system. Cattle adapted using SB had greater DMI than cattle adapted using CON (0.01). As steers were adapted to finishing diets, DMI increased ( = 0.01), average ruminal pH decreased ( = 0.05), and time and area below a pH of 5.6 increased ( ≤ 0.04) for both treatments. Ruminal pH for CON steers decreased from 6.59 to 6.12 across periods as corn replaced alfalfa hay whereas ruminal pH decreased from 6.00 to 5.79 for SB steers. Steers adapted using SB had greater ( ≤ 0.05) in situ digestion of adaptation diets than steers adapted using CON for adaptation periods 3, 4, and 5. The SB diets were more digestible than the CON diets when incubated in either CON- or SB-fed steers for adaptation periods 1 and 2 (0.01). Experiment 2 used 240 finishing steers (273 kg BW [SD 14]) to determine performance impacts of using Sweet Bran instead of forage to adapt cattle to finishing diets. Steers were fed either decreasing Sweet Bran inclusion while increasing corn (SB) or decreasing alfalfa hay inclusion while increasing corn (CON). Treatments were applied only during grain adaptation (26 d) and all steers were finished on a common diet containing 35% Sweet Bran for an additional 147 d. Steers adapted using SB had greater ( ≤ 0.01) final BW, ADG, G:F, and HCW compared with steers adapted using CON, even though treatments differed only the first 26 d. Grain adaptation treatment had no effect ( ≥ 0.13) on carcass quality. These results indicate that Sweet Bran can be used to adapt cattle to finishing diets instead of forage and improves ADG and G:F while decreasing the forage needs of feedlots.

Expansion of the biodiesel industry has increased the crude glycerin (CG) supply. Crude glycerin has the potential of replacing corn in ruminant diets because the glycerol can be converted to glucose in the liver of ruminants, providing energy for cellular metabolism. The objective was to evaluate the effects of CG with urea, soybean meal, cottonseed meal, and corn gluten feed, respectively, on intake, digestibility, microbial protein yield, and efficiency of N utilization. Five Nellore bulls (initial BW of 448 kg [SD 14]) grazing tropical pasture were used in a 5 × 5 Latin square design. The supplements were control (no supplementation; only free-choice mineral mixture ad libitum), CG with urea (CG-Urea), CG with soybean meal, CG with cottonseed meal, and CG with corn gluten. Crude glycerin was used in all supplements to replace corn (15% of DM supplement). There were differences between CG-Urea and other supplements with regard to intake of DM (% of BW and total;0.01), OM (0.01), CP (0.01), and TDN (0.01). The digestibility of CP was greater ( = 0.04) for animals supplemented with CG-Urea than for those fed other supplements. Animals supplemented with CG-Urea showed greater N intake (0.01) and N ammonia ( = 0.04) than those supplemented with other treatments. Nitrogen retained (g/d) was not affected by protein source but was greater for cattle fed a protein supplement compared with cattle fed the control supplement (0.01). Supplementing the animals with protein sources increased ( = 0.02) the daily production of rumen microbial nitrogen (g/d) compared with the control group. Microbial protein (g/d) was lesser for the control than for protein sources ( = 0.02). However, when expressed relative to TDN ( = 0.35) and CP ( = 0.82), there were no differences across treatments. Crude protein intake per digestible OM intake (g CP/kg digestible OM intake) was greater for animals fed protein sources compared with animals fed control supplements (0.01). Based on nutrients intake and microbial protein yield, CG-Urea supplement has a greater feeding value compared with other protein sources. Crude glycerin, when used to replace corn in 15% of DM supplement, may be effective to improved N utilization and microbial protein yield in rumen of Nellore bulls grazing cv. Marandu.

Six experiments were conducted to evaluate dietary cation-anion difference (DCAD) in concentrate diets on urinary pH, feedlot performance, and N mass balance. In Exp. 1, 15 wether lambs (33.5 ± 3.0 kg) in five 3 × 3 Latin squares were fed a basal diet of 82.5% dry-rolled corn (DRC), 7.5% alfalfa hay, 5% molasses, and 5% supplement with different proportions of anionic and cationic salts. The DCAD was -45, -24, -16, -8, 0, +8, +16, +24, +32, and +40 mEq per 100 g of DM with the control basal diet (DCAD = +8) included in each square. Urinary pH increased (cubic, P 0.11) among treatments in either experiment. Efficiency of BW gain was increased (P = 0.05) for steers fed NEG compared with POS in Exp. 5 but was not different (P = 0.11) in Exp. 6. Amount of N intake, retention, excretion, and manure N (kg/steer) were not different (P > 0.11) among treatments in either experiment. Manure pH (soil, feces, and urine) was decreased (P < 0.01) in pens fed NEG compared with POS in both experiments. Amount of N lost (kg/steer) was not different (P = 0.44) in Exp. 5, but tended (P = 0.09) to be 10.6% greater for POS compared with NEG in Exp. 6. Urinary pH was decreased by reducing DCAD, but this had minimal effect on N losses in open feedlot pens in these experiments.

Three experiments were conducted examining the effects of feeding different levels of dried distillers grains (DDG) and different proportions of condensed distillers solubles (CDS) added to DDG on performance and digestibility in forage-fed steers. In Exp. 1, a total of 120 individually fed crossbred steers (276 +/- 31 kg) were used in a randomized complete block design with a 4 x 5 factorial arrangement of treatments. Factors included DDG supplementation level (0.25, 0.50, 0.75, or 1.0% of BW daily) and proportion of CDS in DDG (0.0, 5.4, 14.5, 19.1, and 22.1% of DDG DM). A basal diet of 58.8% alfalfa hay, 39.2% sorghum silage, and 2% vitamin and mineral supplement (DM basis) was fed for ad libitum intake. As the level of DDG increased, intake of forage decreased linearly (P0.01), intake of DDG increased linearly (P0.01), and total DMI increased quadratically (P = 0.06). A DDG level x CDS level interaction (P0.01) was observed for ADG and G:F. The 0.0, 5.4, 14.5, 19.1, and 22.1% CDS treatments had the greatest ADG when DDG was supplemented at 0.75, 1.0, 1.0, 0.75, and 0.50% of BW daily, respectively. In Exp. 2, four crossbred steers (295 +/- 19 kg) were used in a 3-period switchback design. A basal diet of 58.8% alfalfa hay, 39.2% brome hay, and 2% vitamin and mineral supplement (DM basis) was fed at 95% of ad libitum intake. Treatments were DDG containing 0.0 or 22.1% CDS supplemented at 1.0% of BW daily. Apparent total tract digestibility was measured by total fecal collection. No differences between treatments were observed for digestibility of DM, OM, or NDF (P/= 0.14). Digestibility of ether extract was greater (P = 0.02) in steers supplemented with DDG containing 22.1% CDS. In Exp. 3, two ruminally and duodenally cannulated Holstein steers (663 +/- 24 kg) were used to estimate DM and CP digestion of the DDG fed in Exp. 1 using the mobile bag technique. Basal diets were the same as fed in Exp. 1 and steers were supplemented with DDG at 0.5% of BW daily. Ruminal DM digestibility increased linearly (P0.01), and postruminal and total tract DM digestibility increased quadratically (P = 0.02 and P = 0.03, respectively) as the level of CDS increased. Level of CDS may affect growing steer performance because depressions in ADG and G:F were observed as intake of ether extract increased. A clear explanation for the interaction between the DDG supplementation level and the CDS level on growing steer performance was not evident in the digestion experiments.

In a 3-yr study, corn dried distillers grains plus solubles (DDGS) were evaluated as a substitute for forage and N fertilizer in yearling steers grazing smooth bromegrass. A total of 135 steers (330 +/- 10 kg) were used in a randomized complete block design to measure the effects of DDGS supplementation and N fertilization on animal and pasture performance. Steers were initially stocked at 6.8 animal unit month (AUM)/ha on nonfertilized smooth bromegrass pastures (CONT), at 9.9 AUM/ha on smooth bromegrass pastures fertilized with 90 kg of N/ha (FERT), or at 9.9 AUM/ha on nonfertilized smooth bromegrass pastures with 2.3 kg of DDGS DM supplemented daily (SUPP). Paddock was the experimental unit, with 3 replications per year for 3 yr. Paddocks were strip-grazed and put-and-take cattle were used to maintain similar grazing pressure among treatment paddocks during the 160-d grazing season. In vitro DM disappearance declined quadratically (P < 0.01), whereas CP and standing crop showed cubic responses (P < 0.01) throughout the grazing season. Crude protein was greater (P < 0.05) for FERT compared with CONT and SUPP. Standing crop was 18% greater (P < 0.01) for FERT than CONT and was 10% greater (P < 0.01) than SUPP. Adjusted stocking rates (AUM/ha) were greater (P < 0.01) for FERT and SUPP compared with CONT. Final BW were greater (P < 0.01) for SUPP steers compared with CONT and FERT steers. Similar results were observed for ADG, with SUPP steers gaining more (P < 0.01) compared with CONT and FERT steers. Total BW gain per hectare was increased (P < 0.01) by 53% with FERT and by 105% with SUPP. Feedlot ADG was similar among treatments (P = 0.88), and SUPP steers maintained their BW advantage through the finishing phase. Dried distillers grains can be used to substitute effectively for N fertilizer by increasing the performance of yearling steers grazing smooth bromegrass and increasing stocking rates compared with nonfertilized pastures.

A clinical trial conducted during the summer of 2006 evaluated effects of two- and three-dose regimens of an Escherichia coli O157 vaccine product on the probability of detecting E. coli O157:H7 in feces and colonization of the terminal rectum. The three-dose regimen significantly reduced the probability for cattle to shed E. coli O157:H7 in feces 65% compared to placebo-treated cattle. A dose–effect was demonstrated because a two-dose regimen of the vaccine product was intermediate in effect. These results are consistent with previous estimates of vaccine efficacy against fecal shedding, and agree with our previous finding that efficacy of two or three doses of this vaccine product exhibit a dose–response.

A feedlot (Exp. 1) experiment was conducted to evaluate the effects of an essential oil mixture (EOM), experimental essential oil mixture (EXP), tylosin, and monensin (MON) on performance, carcass characteristics, and liver abscesses. A metabolism experiment (Exp. 2) was conducted to evaluate the effects of EOM, EXP, and MON on ruminal fermentation and digestibility in finishing steers. In Exp. 1, 468 yearling steers (398 +/- 34 kg initial BW) were used in 50 pens (10 pens/treatment) and received their respective dietary treatments for 115 d. Five dietary treatments were compared in Exp. 1: 1) control, no additives (CON); 2) EOM, 1.0 g/steer daily; 3) EXP, 1.0 g/steer daily; 4) EOM, 1.0 g/steer daily plus tylosin, 90 mg/steer daily (EOM+T); and 5) monensin, 300 mg/steer daily plus tylosin, 90 mg/steer daily (MON+T). Compared with CON, steers fed MON+T had decreased DMI (P 0.58). There was a trend (P = 0.09) for a treatment effect on 12th-rib fat thickness, which resulted in a significant increase in calculated yield grade for the EOM+T treatment. No other carcass characteristics were affected by treatment (P >/= 0.10). Prevalence of total liver abscesses was reduced for steers fed tylosin compared with no tylosin (P 0.30). Feed intake patterns were similar among feed additive treatments (P > 0.13). Total VFA (P = 0.10) and acetate (P = 0.06) concentrations tended to be affected by treatment with EOM numerically greater than CON. Average ruminal pH ranged from 5.59 to 5.72 and did not differ among treatments. Addition of a EOM or monensin to a diet containing tylosin improves G:F, but little difference was observed in metabolism or digestibility.

Three experiments evaluated the lipids in distillers grains plus solubles compared with corn or other sources of lipid in finishing diets. Experiment 1 utilized 60 individually fed yearling heifers (349 +/- 34 kg of BW) fed treatments consisting of 0, 20, or 40% (DM basis) wet distillers grains plus solubles (WDGS), or 0, 2.5, or 5.0% (DM basis) corn oil in a finishing diet based on high-moisture corn (HMC) and dry-rolled corn. Cattle fed 20 and 40% WDGS had greater (P < 0.10) G:F than cattle fed 0% WDGS. Cattle fed the 5.0% corn oil had less overall performance than cattle fed the other diets. Results from Exp. 1 indicated that adding fat from WDGS improves performance, whereas supplementing 5.0% corn oil depressed G:F, suggesting that the fat within WDGS is different than corn oil. Experiment 2 used 234 yearling steers (352 +/- 16 kg of BW) fed 1 of 5 treatments consisting of 20 or 40% (DM basis) dry distillers grains plus solubles, 1.3 or 2.6% (DM basis) tallow, or HMC. All diets contained 20% (DM basis) wet corn gluten feed as a method of controlling acidosis. No differences between treatments for any performance variables were observed in Exp. 2. The dry distillers grains plus solubles may be similar to tallow and HMC in finishing diets containing 20% wet corn gluten feed. Experiment 3 used 5 Holstein steers equipped with ruminal and duodenal cannulas in a 5 x 5 Latin square design. Treatments were a 40% WDGS diet, 2 composites, one consisting of corn bran and corn gluten meal; and one consisting of corn bran, corn gluten meal, and corn oil; and 2 dry-rolled corn-based diets supplemented with corn oil or not. Cattle fed the WDGS diet had numerically less rumen pH compared with cattle fed other treatments. Cattle fed WDGS had greater (P < 0.10) molar proportions of propionate, decreased (P < 0.10) acetate:propionate ratios, greater (P < 0.10) total tract fat digestion, and a greater (P < 0.10) proportion of unsaturated fatty acids reaching the duodenum than cattle fed other treatments. Therefore, the greater energy value of WDGS compared with corn may be due to more propionate production, greater fat digestibility, and more unsaturated fatty acids reaching the duodenum.

Two experiments determined effects of collection and preparation techniques on nutrient composition of masticate samples from esophageally fistulated cattle. In Exp. 1, 12 esophageally fistulated cattle were maintained on 2 precollection diets, high CP (24% CP; = 6) or low CP (7.7% CP; = 6), for 8 d. On d 9, the esophageal plug was removed, screen bottom bags were attached, and each cow was offered fresh grass. Immediately after fresh grass sample collection was complete, dry grass (hay) was offered and a sample was collected. Blood samples were collected and analyzed for serum urea nitrogen concentration. Masticate samples of both fresh and dry grass were divided and each was either squeezed by hand until no more saliva could be removed or remained unsqueezed. In Exp. 2, 10 esophageally fistulated cattle were fitted with either screen ( = 5) or solid ( = 5) bottom collection bags after removal of the esophageal plug and presented grass hay, fresh grass, alfalfa hay, or fresh alfalfa. In Exp. 1, the precollection diet did not affect ( = 0.49) CP content of masticate even though serum urea nitrogen tended to be greater ( = 0.08) for high- vs. low-CP precollection diets. Forage harvest type offered (fresh vs. hay) interacted ( = 0.01) with preparation technique (squeezed vs. unsqueezed) for CP, where CP decreased in squeezed fresh samples (0.001) but not in squeezed grass hay samples ( = 0.98). In Exp. 2, ingestion greatly increased levels of ash (0.001). Crude protein was greater (0.004) before ingestion for all samples except grass hay ( = 0.43). Levels of NDF were similar before and after ingestion (0.15) for all samples except fresh alfalfa, which was greater after ingestion ( = 0.002). Ingestion status did not affect in vitro OM disappearance (IVOMD;0.34) except for grass hay, which was greater after ingestion (0.001). Bag type (screen vs. solid) did not affect ash and NDF (0.31), except for fresh alfalfa, which were greater (0.03) for solid bottom bags. Bag type did not affect alfalfa CP ( = 0.71) but did affect grass CP, which was lower ( = 0.02) for solid bottom bags. Bag type did not affect IVOMD (0.33). More ( = 0.01) fresh forage than hay was recovered through the esophageal opening. Previous diet did not impact masticate samples but squeezing impacted CP levels of high-quality forage and therefore should not be performed. Nutrient values should be reported on an OM basis.

Two experiments were conducted to determine the effects of roughage source and inclusion in diets containing wet distillers' grains plus solubles (WDGS) on finishing cattle performance and ruminal metabolism. In Exp. 1, 385 crossbred steer calves (initial BW = 346 kg [SD 29]) were used in a finishing trial. A control diet with no roughage inclusion was compared with 6 diets containing either alfalfa hay (ALF), corn silage (CSIL), or corn stalks (CSTK) at 2 inclusions as a 3 × 2 factorial. Alfalfa hay was included at 4 (low) or 8% (standard) of diet DM. Diets containing CSIL or CSTK were formulated to provide total dietary NDF equal to the low and standard ALF inclusion diets. The final diets contained 6.13 and 12.26% CSIL or 3.04 and 6.08% CSTK (DM basis). All diets contained 30% WDGS and a 1:1 mixture of dry-rolled and high-moisture corn (DM basis). Cattle fed no roughage had reduced (0.01) DMI and tended ( ≤ 0.10) to have the lowest final BW and ADG compared with cattle fed roughage. There were no differences ( ≥ 0.11) in DMI, ADG, or G:F due to roughage source. Cattle fed a standard inclusion of roughage had greater ( ≤ 0.04) DMI and ADG compared with cattle fed diets with low inclusion, regardless of roughage source. Feed efficiency tended to be different among treatments ( = 0.09), with cattle fed no roughage having greater G:F than all treatments ( ≤ 0.06) except cattle fed the low level of CSTK, which had a similar G:F ( = 0.48). Feed efficiency was not affected by source of roughage ( = 0.23) or inclusion of roughage ( = 0.49). In Exp. 2, 6 ruminally fistulated steers (347 kg BW [SD 25]) were used in a 6 × 6 Latin square design. Treatments were arranged as a 2 × 3 factorial with ALF or CSTK included at zero, low, or standard levels similar to Exp. 1. Apparent total tract digestibility (%) of DM, OM, and NDF decreased linearly ( ≤ 0.07) due to increasing roughage inclusion. Average, maximum, and minimum ruminal pH increased linearly ( ≤ 0.09) as roughage inclusion was increased. Based on the results of this study, low levels of CSTK improved cattle performance relative to low inclusions of ALF or CSIL. Diets with standard inclusions of ALF, CSIL, or CSTK had similar performance. Roughage sources can be exchanged to provide equal NDF in finishing diets containing 30% WDGS without negatively impacting finishing cattle. Based on ADG, eliminating roughages when 30% WDGS was included in finishing diets was not beneficial.

Two experiments evaluated the effects of condensed distillers solubles (CDS) on performance and carcass characteristics of finishing beef cattle. In Exp. 1, 250 crossbred steers (initial BW = 355 ± 18 kg) were fed 0, 9, 18, 27, or 36% CDS (DM basis) which replaced a portion of urea and a 1:1 ratio of dry-rolled corn (DRC) and high-moisture corn (HMC). Steers were divided into 3 BW blocks and were assigned randomly to 25 pens. Dietary fat increased from 3.7 to 9.4% as CDS inclusion increased from 0 to 36%. Intake decreased linearly (0.01) as CDS increased. A quadratic response was observed for ADG ( = 0.01) and G:F (0.01) with maximum gain calculated at 20.8% CDS and maximum G:F at 32.5% CDS inclusion, which was 12% more efficient than those fed 0% CDS. Experiment 2 was designed as a 2 × 4 factorial using 400 crossbred steers (initial BW = 339 ± 15 kg) evaluating 0, 7, 14, or 21% CDS (DM basis) in 2 base byproduct diets containing either 20% modified distillers grains plus solubles (MDGS) or 20% Synergy (a blend of wet corn gluten feed and MDGS). Steers were divided into 2 BW blocks and were assigned randomly to 40 pens. A tendency for a base diet × CDS inclusion interaction was observed for ADG, HCW, and final BW (0.10). Gain increased linearly ( = 0.01) and tended to increase quadratically ( = 0.09) in MDGS diets, with maximum calculated ADG at 16% CDS inclusion. Inclusion of CDS had no effect on ADG in Synergy-based diets. Increasing CDS resulted in a linear increase in G:F (0.01) regardless of basal diet. Condensed distillers solubles may be included in the diet at greater than 30% (DM basis) without other byproducts and improve animal performance. Likewise, CDS can be fed in combination with other byproduct feeds but with less improvement in performance.

Twelve 2-ha, Nebraska Sandhills upland range paddocks were used in a 2-yr study to determine effects of stocking rate on grazed forage nutrient value in early summer. Paddocks contain a mixture of native cool- and warm-season grasses with forbs as a minor component. Stocking rates were 0 (control), 0.57 (light), and 0.85 (heavy) animal unit months per ha, respectively. Three esophageally fistulated cows collected diet samples on May 14 (d 0), May 21 (d 7), May 28 (d 14), and June 4 (d 21) in 2013 and 2014. Ten quadrats per paddock were clipped and separated into current or previous year growth on each diet sampling date. All samples were analyzed for CP, NDF, and in vitro OM disappearance, which was adjusted to an in vivo OM basis (). For diet samples, treatment interacted (0.001) with sampling date for CP, NDF, and IVOMD. However, treatment and date did not interact ( ≥ 0.32) for clipped samples. Diets collected in control paddocks had greater (0.05) IVOMD and CP and lower NDF compared with light and heavy stocking rate paddocks on d 7, 14, and 21 but light stocking rate paddocks did not differ ( ≥ 0.26) from heavy stocking rate paddocks on any sampling day except d 21 NDF ( = 0.03). In general, previous year growth IVOMD, CP, and NDF were not affected ( ≥ 0.11) by treatment. Generally, current year growth IVOMD and CP were not affected ( ≥ 0.22) by treatment. Current year growth NDF did not differ ( = 0.23) among stocking rates on d 0, but control paddock had lower ( = 0.02) NDF than light and heavy on d 7, 14, and 21. In stocked paddocks, diet samples had greater (0.01) IVOMD and CP and lower NDF than current and previous year growth except IVOMD on d 0 where diet and current year growth did not differ ( = 0.34). Generally, in control paddocks, current year growth and diet samples had greater (0.01) IVOMD and CP than previous year growth. Control paddocks had greater (0.01) forage accumulation than stocked paddocks on d 7, 14, and 21; however, light and heavy stocked paddocks did not differ ( ≥ 0.29). On d 0 it was estimated that 96% of the diet was current year growth and only 4% previous year growth, whereas on d 21, 70% of the diet was current year growth vs. 30% previous year growth. Stocking pastures decrease current year growth forage mass and therefore diet nutritive value by forcing cattle to consume diets containing previous year growth in early summer.

Two studies were conducted to optimize use of alkaline-treated corn stover and wheat straw and distillers grains as partial corn replacements. In Exp. 1, a finishing experiment used 30 pens (12 steers/pen) of calf-fed steers (initial BW = 374 ± 23.9 kg) with a 2 × 2 + 1 factorial arrangement of treatments with 6 replications per treatment. Factors were grind size, where corn stover was processed through a 2.54- or 7.62-cm screen, and chemical treatment (corn stover either fed in native, non-treated form [NT; 93.4% DM] or alkaline treated [AT; 5% CaO hydrated to 50% DM]). No interactions (P ≥ 0.38) were noted between grind size and chemical treatment. Feeding AT compared with NT improved (P ≤ 0.02) final BW, ADG, and G:F. Reducing grind size improved (P ≤ 0.01) ADG and G:F, and no interaction with chemical treatment was observed. Steers fed AT had similar DMI, ADG, G:F, and carcass characteristics compared with a 5% roughage control that contained 15 percentage units (DM basis) more corn. In Exp. 2, 60 individually fed steers (initial BW = 402 ± 61.4 kg) were randomly assigned to 10 diets. Six treatments evaluated 10, 25, or 40% dry-rolled corn (DRC), which was replaced with either a 2:1 or 3:1 ratio (DM basis) of modified distillers grains plus solubles (MDGS) and treated corn stover analyzed as a 2 × 3 factorial. An additional 3 treatments were added where a 3:1 ratio of MDGS:straw were compared with a 3:1 ratio of MDGS:stover. As DRC increased, G:F (P = 0.06) quadratically increased for 3:1 MDGS:stover diets. Increasing DRC increased (P = 0.07) G:F in treated stover diets, regardless of ratio. Increasing DRC increased (P = 0.10) ADG for 3:1 ratios for both straw and stover. Reducing grind size, feeding a maximum of 20% treated crop residue, and maintaining at least 25% corn in the diet are strategies for optimizing cattle performance when replacing dry-rolled and high-moisture corn with treated crop residues and distillers grains.

Increased corn prices over the past decade have altered land use away from traditional forage in favor of corn. Accordingly, beef and dairy producers have had to adopt nontraditional forage resources into their production systems, many of which have become available as a result of increased corn production. Corn residues have become more available due to increases in corn hectares and yield. The individual plant components (i.e., husk, leaf, and stem) vary in fiber digestibility (NDF digestibility estimates = 40.5, 31.4, and 0.6% ± 0.8 for husk, leaf, and stalk, respectively). Stocking cattle to consume 3.6 kg forage/25.5 kg of grain allows cattle to graze selectively; selection of husks and leaves improves cattle performance. Byproducts of the wet and dry milling industries can be supplemented to calves grazing corn residues to provide protein and energy. Optimal gains were observed when these byproducts were supplemented at approximately 2.5 kg/d to 250-kg growing calves. Gestating beef cows do not require supplemental inputs when grazing corn residue, if stocked appropriately. Alkaline treatment of crop residues improves their feeding value. Concentrations of up to 20% harvested corn residue treated with calcium oxide can be included in finishing diets with an average of 1.3% reduction in G:F when diets contain 40% wet or modified distillers grains. Conversely, when untreated corn residues are included in similar finishing diets, G:F is reduced by 13.4%. Calcium oxide-treated residues included in beef growing diets increases DMI and ADG without significant improvements in G:F. Calcium oxide treatment of corn residues has been evaluated in dairy diets by replacing corn or corn silage with variable results. Efficient use of nontraditional fiber sources, such as corn milling byproducts and corn residue, are critical to the future viability of ruminant animal production.

Two studies were conducted to identify methods for treating crop residues to improve digestibility and value in finishing diets based on corn grain and corn wet distillers grain with solubles (WDGS). In Exp. 1, 336 yearling steers (initial BW 356 ± 11.5 kg) were used in a 2 × 3 + 1 factorial arrangement of treatments with 6 pens per treatment. Factors were 3 crop residues (corn cobs, wheat straw, and corn stover) and 2 treatments where crop residues were either fed (20% diet DM) in their native form (NT) or alkaline treated with 5% CaO (DM basis) and hydrated to 50% DM before anaerobic storage (AT). Intakes were not affected by diet (F test; P = 0.30). An interaction between chemical treatment and residue (P0.01) was noted for final BW, ADG, G:F, and HCW. Greater final BW was observed for treated stover (4.6%) and straw (5.6%) compared with NT residues; however, AT and NT cobs were similar. Treated straw (9.7%) and stover (12.5%) resulted in greater ADG (P0.01) and improved G:F (10.7% and 5.0%, respectively; P0.01) compared with NT forms. In Exp. 2, ruminally fistulated steers (n = 5) were used in an unbalanced 5 × 7 incomplete Latin square design with a 2 × 3 + 1 factorial arrangement of treatments. Factors were crop residue (corn cobs, wheat straw, and corn stover) and chemical treatment (NT or AT) fed at 25% of diet DM. Greater DM (73.7% vs. 66.1%; P0.01), OM (77.0% vs. 68.5%; P0.01), fat (89.2 vs. 85.2; P = 0.02), and NDF (66.8% vs. 51.5%; P0.01) digestibilities were noted for AT than for NT. However, no difference (P0.10) was observed between control (46% corn; DM basis) and AT (31% corn; DM basis) for DM digestibility (70.7% vs. 73.7%) or OM digestibility (72.1% vs. 77.0%). Dry matter intakes were not different between treated and untreated diets (P = 0.38), but lower (P0.01) NDF intake was observed for treated diets (3.1 vs. 3.5 kg/d), suggesting that CaO treatment was effective in solubilizing some carbohydrate. These data suggest that 15% replacement of corn and 10% untreated residue with treated forage result in a nutrient supply of OM similar to that of the control. The improvements in total tract fiber digestibility that occurred when treated forages were fed may have been related to increased digestibility of recoverable NDF and not to increased ruminal pH. Feeding chemically treated crop residues and WDGS is an effective strategy for replacing a portion of corn grain and roughage in feedlot diets.

Nitrogen losses from outdoor feedlots are an important environmental issue facing beef producers. Two methods that may lower N losses are cleaning pens more frequently to prevent exposure of manure N during collection on pen surfaces or increasing the C:N ratio of manure by increasing organic matter (OM) on the pen surface. Feeding diets lower in OM digestibility or directly adding OM to pen surfaces may increase the C:N ratio and decrease N losses. In Exp. 1, calves in the winter/spring or yearlings in the summer were fed diets lower in digestibility (BRAN) or fed in pens with sawdust additions (SAWDUST) to increase the C:N ratio and OM on the pen surface. These two treatments were compared to conventional feeding and pen management systems (CONTROL). While decreasing digestibility did depress performance as measured by feed efficiency, feeding BRAN did increase OM on the pen surface and decreased N losses compared to CONTROL in the winter/spring but did not affect N losses or increase manure N during the summer. Adding SAWDUST directly to pens yielded similar results to BRAN, with decreased losses in the winter/spring and little effect during the summer compared to CONTROL. However, when manure was composted, N recovery during composting was increased for both the BRAN and SAWDUST treatments compared to CONTROL suggesting that OM may decrease N losses when manure is composted. In Exp. 2, diets similar to CONTROL and BRAN were evaluated as a 2 X 2 factorial treatment design experiment. The other factor evaluated was cleaning frequency. Pens were either cleaned monthly or cleaned once at the end of the winter/spring feeding period. Performance of steers was similar to results in Exp. 1, with lower feed efficiency for cattle fed BRAN compared to the CONTROL treatment. Dietary treatment and cleaning frequency treatments interacted for N balance in the feedlot. Nitrogen losses were decreased and manure N increased for cattle fed BRAN compared to CONTROL if pens were clean monthly. If pens were not cleaned until the end of the feeding period, diet had little effect on N losses. Interestingly, N losses were similar between both cleaning frequency treatments for cattle fed CONTROL. In Exp. 3, 54 pens were used to evaluate the impact of monthly cleaning on N removal in manure during the summer months. The same diet was fed in all pens, resulting in similar performance across treatments. Cleaning pens monthly increased the amount of manure N removed per steer by 3.74 kg or 66.2% compared to pens cleaned once at the end of the feeding period. These data suggest that cleaning pens more frequently and adding OM to pen surfaces or compost may decrease N losses from outdoor feedlot pens. Treatment responses appear to be dependent on ambient temperature or season, suggesting that future research needs to address both summer and winter/spring feeding periods typical of beef cattle operations.

Cattle weights can be highly variable and are influenced by many factors, including time of weighing, ambient temperature, feed intake, and cattle handling. A protocol of limit feeding has been in use since the 1980s that was designed to reduce variation in gut fill due to differences in intakes. Cattle are penned and fed a 50% hay, 50% wet corn gluten feed or grain diet (DM basis) at an estimated 2% of BW for at least 5 d, after which weights are taken on 2 consecutive d and averaged for a limit-fed BW (LFW). For this analysis, full-fed weights (FFW) also were taken before the limit-feeding period while cattle had ad libitum intakes. Data from 18 experiments were used to analyze differences within 2-d LFW and between LFW and FFW. For 10 of the 18 experiments, FFW also were measured on 2 consecutive d. Cattle included in this summary were grazing cornstalks, smooth bromegrass pasture, Bermuda grass pasture, fescue pasture, native range, or in a dry lot on a 70% forage diet. The largest differences between FFW and LFW for individual cattle were -39 to +44 kg over all 18 experiments. Differences between 2 consecutive d of LFW were -23 to +24 kg for all 18 experiments. Differences between 2 d of FFW were -14 to +34 kg in the 10 experiments measuring FFW on 2 consecutive d. There was not a clear relationship between FFW and LFW; each weighing scenario had unique environmental conditions that led to different relationships. Differences in both beginning and ending BW were compounded when calculating ADG. Average daily gain was calculated for 15 of the experiments on the basis of either LFW or FFW. Differences between LFW and FFW ADG were -0.29 to +0.31 kg/d. The maximum ADG based on FFW was 1.62 kg/d. This large ADG, on a forage based diet, was likely due to changes in gut fill rather than tissue gain. These data suggest that handling cattle in a similar manner when weighing is more important than limiting intakes to decrease variance between weights. However, limiting intake before collection of beginning and ending BW better estimates empty body weight of cattle, allowing for a more accurate determination of actual body tissue weight gain. Measuring weights accurately becomes especially crucial when evaluating multiple components within a system (e.g., cornstalks to pasture to feedlot). Feeding a standard diet between these components of the system minimizes differences in gut fill due to treatment and allows for a more accurate determination of each component's contribution to the total system.

Effects of S from wet or dry distillers grains with solubles (DGS) containing 0.82 or 1.16% S on animal growth performance, carcass characteristics, apparent total tract digestibility, and ruminal parameters were evaluated. In Exp. 1, crossbred beef steers (n = 120; 345 ± 34 kg BW) were individually fed ad libitum using Calan gates. Treatments were applied as a 2 × 2 × 3 + 1 factorial treatment arrangement with factors of DGS type (wet or dry), S content in DGS (0.82 or 1.16% DM basis), and DGS inclusion (20, 30, and 40%, DM basis), as well as a corn control diet (no DGS). In Exp. 2, ruminally cannulated crossbred beef steers (n = 6; 381 ± 31 kg BW) were assigned to 1 of 5 diets in a 5 × 6 unbalanced Latin Square design and fed ad libitum through five 14-d periods. A 2 × 2 + 1 factorial treatment arrangement was used with the factors of DGS type and S content in DGS (similar to Exp. 1). Inclusion of DGS was 40%, except for a MATCH diet containing wet 1.16% S DGS included at 31.4% (DM basis). Intake of DM decreased linearly (P0.01) and quadratically (P0.01) for steers fed wet and dry DGS that was 1.16% S, respectively. In addition, steers fed dry DGS consumed 9% more DM (P0.01) than those fed wet. Gain decreased linearly (P = 0.02) when wet 1.16% S DGS increased in the diet, representing a 12% drop in ADG between the Control and 40% DGS inclusion. A quadratic (P = 0.02) improvement in G:F was observed for steers fed wet DGS compared with dry, regardless of S content (P = 0.52). Feeding diets with wet 1.16% S DGS linearly decreased (P = 0.03) HCW. In Exp. 2, molar proportion of propionate declined (P = 0.01) 9% and A:P ratio tended (P = 0.13) to be greater when 1.16 compared with 0.82% S DGS was fed. Apparent total tract DMD was not affected (P0.16) and only subtle changes (P0.01) in ruminal pH parameters were observed. Greater (P = 0.02) ruminal H2S concentration for steers fed wet compared with dry DGS was observed, while 1.16% S DGS tended (P = 0.12) to produce greater ruminal H2S than 0.82% S. Sulfur in wet DGS appears to be more prone to be converted to ruminal H2S, because feeding 1.16% S as wet DGS had a greater impact on ADG, DMI, and ruminal H2S compared with dry DGS.

Effects of organic and inorganic sources of S on intake, intake pattern, ruminal pH, VFA profile, and ruminal H2S gas concentration ([H2S]) were evaluated, which lead to development of a procedure to measure ruminal S availability for reduction [ruminal available S (RAS)] as well as compare with an estimated number [adjusted ruminal protein S (ARPS)]. Ruminally cannulated crossbred beef steers (n = 5; BW = 548 ± 46 kg) were assigned to 1 of 5 diets in a 5×5 Latin square design and fed ad libitum in five 21-d periods. Steers were fed a dry-rolled corn diet (CON), inorganic S source (ammonium sulfate; INORG), organic S source (corn gluten meal) fed at 9.8 (ORG-L) or 23% of diet DM (ORG-H), or wet distillers grains with solubles (WDGS) fed at 50% of diet DM. For the laboratory procedure, individual ingredients were incubated with ruminal fluid from heifers fed 60% corn-based diets (n = 2) and McDougall's buffer. Bottles were cooled in ice, centrifuged, and decanted, and the precipitate was analyzed for S. Steers fed INORG tended (P = 0.12) to consume 12% less DM. Total S intake was greater (P0.01) for steers fed WDGS (60 g/d) followed by ORG-H, and the lowest S intake was observed for CON (22 g/d). Intakes of ARPS and RAS were greater (P0.01) for steers fed WDGS followed by INORG, ORG-H, ORG-L, and CON diets. Steers fed WDGS and INORG diets spent 13% more time eating (P0.01) compared with other treatments. There was an interaction (P = 0.05) between treatment and time for ruminal [H2S]. Similar [H2S] were observed for steers fed INORG and WDGS diets (P = 0.28), which were greater (P ≤ 0.05) than other treatments. Greater ruminal [H2S] at 8 h compared with 13 h postfeeding was observed for steers fed ORG-H, ORG-L, and CON diets (P ≤ 0.04). Nearly 65% of ruminal [H2S] variation was explained (linear; P0.01) by RAS intake, ARPS explained 58% (linear; P0.01), S intake explained 29% (quadratic; P0.01), average ruminal pH explained 12% (linear; P0.01), and area below ruminal pH 5.6 explained 16% (linear, P0.01) of the variation. A 6% decrease in acetate (P = 0.01), 20% increase in propionate molar proportions (P = 0.02), and a lower acetate:proprionate ratio (P = 0.02) were observed for steers fed INORG compared with CON diet. The RAS concept is important for predicting ruminal [H2S] rather than just total S in the diet. Coefficients of RAS for individual ingredients can be predicted using in vitro procedures. Ruminal [H2S] may also modulate intake pattern.

Four experiments were conducted to evaluate RUP content and digestibility for smooth bromegrass, subirrigated meadow, upland native range, and warm-season grasses. Samples were collected from esophageally cannulated cows or ruminally cannulated steers. Forages were ruminally incubated in in situ bags for durations of time based on 75% of total mean retention time, which was based on IVDMD and rate of passage calculations. One-half of the bags were duodenally incubated and excreted in the feces, and NDIN was analyzed on all bags for RUP calculations. Crude protein was numerically greater early in the growing cycle for grasses compared with later as grasses matured (P ≤ 0.32). The RUP was 13.3%, 13.3%, and 19.7% of CP for smooth bromegrass, subirrigated meadow, and upland native range, respectively. These values tended to be lower early in the growth cycle and increased (linear P ≤ 0.13) as forages matured for warm-season grasses and subirrigated meadows. Because both CP and RUP content change throughout the growing season, expressing RUP as a percentage of DM gives more consistent averages compared with RUP as a percentage of CP. Coefficient of variation values for RUP as a percentage of DM averaged 0.21 over all 4 experiments compared with 0.26 for RUP as a percentage of CP. Average RUP as a percentage of DM was 2.03%, 1.53%, and 1.94% for smooth bromegrass, subirrigated meadow, and upland native range, respectively. Total tract indigestible protein (TTIDP) linearly increased with maturity for subirrigated meadow samples (P0.01). A quadratic response (P ≤ 0.06) for TTIDP was observed in smooth bromegrass and warm-season grass samples. Digestibility of RUP varied considerably, ranging from 25% to 60%. Subirrigated meadow, native range, and smooth bromegrass samples tended to have linear decreases (P ≤ 0.11) in RUP digestibility throughout the growing season. The amount of digested RUP was fairly consistent across experiments and averages for smooth bromegrass, subirrigated meadow, and upland native range were 0.92%, 0.64%, and 0.49% of DM, respectively. Warm-season grasses in Exp. 2 had greater RUP (4.31% of DM) and amount of RUP digested (2.26% of DM), possibly because of cattle selecting for leadplant that contains more CP than the grasses. Forages can vary in CP, RUP, TTIDP, and RUP digestibility depending on the forage type, year, and time within year, but RUP digestibility is likely less than what previous sources have reported.

A total of 3,632 crossbred steers were used in 3 separate randomized complete-block designed finishing experiments. Data from Exp. 1 were analyzed separately whereas data were combined for Exp. 2 and 3, based on corn processing method used [Exp.1 = equal combination of dry-rolled and high-moisture (DRC:HMC); Exp. 2 and 3 = steam-flaked (SFC)]. Steers were fed 1 of 5 treatments to evaluate the effects of monensin and tylosin in feedlot diets containing 25% corn wet distillers grains with solubles (WDGS; DM basis). Treatments included: 1) corn-based diet (no WDGS) with 360 mg/d monensin and 90 mg/d tylosin (CORN+MT), 2) 25% wet distillers grains with solubles (WDGS-CON), 3) 25% WDGS with 360 mg/d monensin (WDGS+M), 4) WDGS with monensin and tylosin at same levels as treatment 1, and 5) WDGS with 480 mg/d monensin and 90 mg/d tylosin (WDGS+HIMT). In Exp. 1, WDGS+MT increased (P0.01) ADG (6.5%), G:F (6.9%), and HCW (3.0%) compared with CORN+MT. Alternatively, in Exp. 2 and 3, WDGS+MT had no effect on ADG (P = 0.18), decreased (P0.01) G:F by 3.2%, and did not affect HCW (P = 0.57) compared with CORN+MT. In Exp. 1, addition of monensin to a WDGS diet increased G:F by 3.1% (P = 0.03) and tended to increase G:F in Exp. 2 and 3 (P = 0.09) compared with WDGS-CON. For all experiments, addition of monensin and tylosin in a diet containing WDGS increased G:F (P0.01) and reduced total and severe liver abscesses (P0.01) compared with WDGS-CON. Additionally, HCW was increased in Exp. 2 and 3 (P0.01) and tended to increase in Exp. 1 (P = 0.09) when monensin and tylosin were fed in a WDGS diet compared with WDGS-CON. Feeding WDGS+MT reduced total liver abscesses by 79.3% (Exp. 1) and 57.6% (Exp. 2 and 3) compared with WDGS-CON. Compared with WDGS+MT, minimal differences were observed when monensin was fed at 480 mg/steer daily with tylosin in diets containing WDGS. Inclusion of WDGS in finishing steer diets did not alter effectiveness of monensin with tylosin in improving G:F and reducing prevalence of liver abscesses, regardless of corn processing method. Corn processing method appears to be an important factor in performance response to WDGS with feeding value of WDGS, measured as an increase in feed efficiency, being greater in a DRC:HMC-based diet compared with a SFC-based diet.

Two calf corn-residue grazing trials were conducted to evaluate the effect of supplementing with two alfalfa hays (Medicago sativa), varying in their amount of CP and ADF, with and without escape protein (EP). In Trial 1, heifers (204 kg) grazed (1.36 heifers/ha) non-irrigated fields for 92 d. No difference (P > .05) in ADG was found when medium-protein (16.3% CP) and high-protein (18.0% CP) alfalfa hays were provided at 2.7 kg of DM.heifer-1.d-1. In Trial 2, 60 steers (257 kg) were supplemented individually with medium-protein (17.6% CP) alfalfa hay, 1.86 (MPL) and 2.27 kg DM (MPH), and one level of high-protein (18.7% CP) alfalfa hay, 1.86 kg DM (HPL). In a 2 x 3 factorial arrangement of treatments, steers were fed with or without EP (113 g.steer-1.d-1 from blood meal and corn gluten meal). Steers grazed a non-irrigated corn residue field (2.58 steers/ha) for 57 d and were watered and individually supplemented overnight. Diet quality and composition was estimated by collecting extrusa samples twice each week using four esophageally fistulated steers. No effects of alfalfa protein content or level (P > .05) were reflected in gain: 357, 309, and 326 g.steer-1.d-1 for steers receiving MPL, MPH, or HPL alfalfa treatments, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

Two experiments using 96 steers each were conducted to evaluate the effect of corn wet distillers grains plus solubles (WDGS) concentration on steer performance, N loss, and P mass balance. Feeding WDGS as an energy source instead of protein may increase N release into the environment but also the amount of N removed in the manure. Calves (BW = 294 ± 33 kg) were fed 167 d from November to May (WIN), and yearlings (BW = 373 ± 24 kg) were fed 133 d from June to October (SUM). Treatments consisted of 0, 15, and 30% dietary inclusion of WDGS (DM basis) replacing corn (CON, 15WDGS, 30WDGS, respectively). Basal diets consisted of high-moisture and dry-rolled corn fed at a 1:1 ratio, 7.5% alfalfa hay, 5% molasses, and 5% supplement (DM basis). The CON and 15WDGS diets were formulated to meet MP requirements, and 30WDGS exceeded MP requirements. Dry matter intake, ADG, and HCW increased linearly (P0.05) with WDGS concentration in the WIN, whereas DMI and ADG increased linearly (P0.10) in the SUM. Efficiency of BW gain was not different (P0.10) among treatments in either experiment. Nitrogen and P intake increased linearly (P0.01) with WDGS concentration in both experiments. Calculated retention of N and P increased linearly (P ≤ 0.05) with WDGS concentration in the WIN but not in the SUM (P0.10). Calculated excretion of N and P increased linearly (P0.01) with WDGS concentration in both experiments. Amount of N removed in the manure was not different (P = 0.26) among treatments in the WIN but increased linearly (P = 0.05) with WDGS concentration in the SUM. Amount of P and OM removed increased linearly (P ≤ 0.05) with WDGS concentration in both experiments. Amount of N lost (kg/steer) increased linearly (P0.05) with WDGS concentration in both experiments. Expressed as a percentage of N excretion, N volatilization rate (amount of N lost divided by N excretion) was not different (P0.30) among treatments and averaged 68.3 and 77.0 in the WIN and SUM, respectively. More N volatilized when WDGS were fed, but not all of the additional N excreted was volatilized. Regressing the amount of OM on the pen surface against manure N, 98% of the variability for manure N in the WIN and 92% in the SUM was accounted for. Feeding WDGS increased the total amount of N lost to volatilization; however, not all of the additional N excreted was lost because of an increase in the proportion of manure OM.

Six experiments were conducted to evaluate dietary cation-anion difference (DCAD) in concentrate diets on urinary pH, feedlot performance, and N mass balance. In Exp. 1, 15 wether lambs (33.5 ± 3.0 kg) in five 3 × 3 Latin squares were fed a basal diet of 82.5% dry-rolled corn (DRC), 7.5% alfalfa hay, 5% molasses, and 5% supplement with different proportions of anionic and cationic salts. The DCAD was -45, -24, -16, -8, 0, +8, +16, +24, +32, and +40 mEq per 100 g of DM with the control basal diet (DCAD = +8) included in each square. Urinary pH increased (cubic, P0.01) as DCAD increased and DMI increased linearly (P0.01) with increasing DCAD. In Exp. 2 and 3, 8 Holstein steers (312 ± 24 kg) were used in 2 consecutive 4 × 4 Latin squares. Steers were fed either the same basal diet as Exp. 1 or a basal diet with 20% wet distillers grains (WDGS) replacing DRC. In Exp. 2, DCAD was adjusted to -2, -12, and -22 mEq per 100 g of DM from the basal diet (DCAD = +8) and DCAD was adjusted in Exp. 3 to -12, -22, and -32 mEq per 100 g of DM from the basal WDGS diet (DCAD = -2). Urinary pH decreased linearly as DCAD decreased (P0.01) in both experiments, whereas DMI decreased linearly in Exp. 2 (P = 0.02) but not Exp. 3 (P = 0.96). In Exp. 4, 6 crossbred steers (373 ± 37 kg) were used in a 2-period crossover design. Steers were fed the same basal diet as Exp. 3 with DCAD of -16 (NEG) and +20 (POS) mEq per 100 g of DM. Urinary pH and DMI (P0.05) were less for cattle fed the NEG diet compared with POS. In 2 experiments, steers (n = 96 each) were fed NEG or POS as calves (260 ± 22 kg of BW) for 196 d from November to May (Exp. 5) or as yearlings (339 ± 32 kg of BW) for 145 d from June to October (Exp. 6). Final BW, DMI, ADG, and HCW were not different (P0.11) among treatments in either experiment. Efficiency of BW gain was increased (P = 0.05) for steers fed NEG compared with POS in Exp. 5 but was not different (P = 0.11) in Exp. 6. Amount of N intake, retention, excretion, and manure N (kg/steer) were not different (P0.11) among treatments in either experiment. Manure pH (soil, feces, and urine) was decreased (P0.01) in pens fed NEG compared with POS in both experiments. Amount of N lost (kg/steer) was not different (P = 0.44) in Exp. 5, but tended (P = 0.09) to be 10.6% greater for POS compared with NEG in Exp. 6. Urinary pH was decreased by reducing DCAD, but this had minimal effect on N losses in open feedlot pens in these experiments.

Two trials were conducted to determine and evaluate the rumen degradable and escape protein (EP) value of two summer annuals for yearling cattle. In Trial 1,120 heifers (Bos taurus) (530 lb), arranged in a completely randomized design, were supplemented with 0, 0.25, 0.40, or 0.55 lb crude protein (CP)/d supplied by corn gluten meal:blood meal (CGM:BM) replacing a corn starch:molasses control, keeping the supplements equivalent in energy. Heifers grazing ‘Piper’ sudangrass [Sorghum bicolor (L.) Moench] (70 d) showed a negative linear (P < 0.02) response to supplemental protein and quadratic (P < 0.10) response (1.41,1.54,1.32, and 1.14 lb/d gain, respectively). Heifers grazing Northrup King ‘Millex’ pearl millet [Pennisetum americanum (L.) Leeke] (55 d) showed a cubic (P < 0.05) response (1.01, 1.23, 1.08, 1.25 lb/d gain, respectively) which tended to be linear (P = 0.13). Cattle on pearl millet responded to supplemental protein while cattle on sudangrass did not, which is supported by high EP values of sudangrass extrusa. In Trial 2, 60 Angus heifers and 60 Angus steers (600 lb) grazing sudangrass (56 d) were allotted to (i) molasses (ii) corn starch (iii) CGM:BM at 0.25 lb CP/d (iv) corn starch and CGM:BM at 0.25 lb CP/d, or (v) CGM:BM at 0.50 lb CP/d. All five treatments contained the same amount of molasses, and corn starch provided energy equal to CGM:BM. Supplemental protein improved gains (P = 0.10) (1.10,0.99,1.14 lb/d, respectively) over the molasses control (0.84 lb/d) but did not increase gains over the corn starch (1.17 lb/d). The lack of response to supplemental EP above the corn starch is again supported by high EP values of the sudangrass extrusa. Research QuestionSummer annuals can provide alternate pastures for grazing yearling cattle during summer slump periods of cool season perennial forages. They are also an alternative crop for cultivated land less suitable (or less profitable) for other cropping systems. Summer annuals can be grazed more intensely than perennial forages because perennial stands must be maintained for subsequent years. For the summer annuals to be a viable alternative, however, they should provide high gains per acre. This can be achieved if digestibility and protein levels are adequate. The objective of Trial 1 (1989) was to determine the escape protein value of sudangrass and pearl millet for growing calves. The objective of Trial 2 (1990) was to further evaluate the metabolizable protein value of sudangrass. Literature SummaryMetabolizable protein is the combination of microbial protein synthesized from rumen degradable protein and escape protein (not degraded in the rumen and used directly by the animal). Metabolizable protein should be adequate for optimum cattle growth before the forage is a viable option. The protein requirement of rapidly growing ruminants is not met by microbial protein synthesis alone. Dietary escape protein has increased performance in growing cattle when energy and ammonia were not limiting microbial protein synthesis. The metabolizable protein value of sudangrass and pearl millet for growing calves has not been evaluated. Study DescriptionIn Trial 1, 60 heifers grazed ‘Piper’ sudangrass (70 d) and 60 heifers grazed Northrup King ‘Millex’ pearl millet (55 d). Treatments: Corn starch:molasses control at 0 lb crude protein (CP)/d Corn gluten meal:blood meal (CGM:BM) at 0.25 lb CP/d CGM:BM at 0.40 lb CP/d CGM:BM at 0.55 lb CP/d In Trial 2, 60 heifers and 60 steers grazed Piper sudangrass (56 d). Treatments: Molasses Corn starch CGM:BM at 0.25 lb CP/d Corn starch and CGM:BM at 0.25 lb CP/d CGM:BM at 0.50 lb CP/d All five treatments contained the same amount of molasses; and corn starch provided energy equivalent to that of CGM:BM. Applied QuestionDid supplemental escape protein increase gains of cattle grazing sudangrass or pearl millet? Supplemental escape protein did not increase gains of cattle grazing sudangrass. The cattle primarily ate leaves which were highly digested. The sudangrass leaves appeared to supply enough escape protein. Supplemental escape protein slightly increased gains of cattle grazing pearl millet. The pearl millet leaves were also highly digested but did not supply adequate escape protein; however, supplementation might not improve gains enough to be economical. Is metabolizable protein limiting in sudangrass? The lack of response to supplemental protein above the corn starch control and the adequate levels of rumen ammonia measured, suggests metabolizable protein is not limiting for growing calves.

In a 3-yr study, 135 crossbred steers (330 ± 10 kg) were used in a randomized complete block design to evaluate corn dried distillers grains plus solubles (DDGS) fed to yearling steers as a substitute for forage and N fertilizer and its effect on N use efficiency in yearling steers grazing smooth bromegrass pastures. Steers were initially stocked at 6.8 animal unit months (AUM)/ha on nonfertilized smooth bromegrass pastures (CONT), at 9.9 AUM/ha on smooth bromegrass pastures fertilized with 90 kg of N/ha (FERT), or at 9.9 AUM/ha on nonfertilized smooth bromegrass pastures with 2.3 kg (DM) of DDGS supplemented daily per steer (SUPP). Paddock was the experimental unit, with 3 replications per treatment per year for 3 yr. Paddocks were strip-grazed, and put-and-take cattle were used to maintain similar grazing pressure among treatment paddocks during the 160-d grazing season. Steers consumed less forage (P0.01), but total N intake for SUPP was greater (P0.01) per steer and per hectare than for FERT, and both were greater (P0.01) than for CONT. Nitrogen retention for steers in the SUPP treatment was increased (P0.01) by 31% compared with N retention in the CONT and FERT treatments. Nitrogen retention per hectare for SUPP was 30 and 98% greater (P0.01) than N retention per hectare for FERT and CONT, respectively. Nitrogen excretion per steer and per hectare were also greater (P0.01) for SUPP than FERT, and both were increased (P0.01) compared with CONT. Animal N use efficiency was similar (P = 0.29) for steers in the CONT, FERT, and SUPP treatments. However, system-based N use improved (P0.01) by 144% for SUPP compared with FERT. The DDGS increased N intake and N excretion in yearling steers. However, because of improvements in BW gain and increases in stocking rate of pastures, DDGS can be a useful tool to increase the efficiency of N use in smooth bromegrass grazing systems.

Phosphorus is an expensive nutrient to supplement, and excess may lead to manure P challenges. Therefore, minimizing dietary P to meet requirements is important. Two experiments were conducted to determine the P requirement of finishing cattle (Exp. 1) and to evaluate the effects of feeding different P concentrations on the quantity and route of P excretion (Exp. 2). In Exp. 1, 60 heifers (BW = 278 kg +/- 17 kg) were individually fed 1 of 5 dietary P concentrations (0.10, 0.17, 0.24, 0.31, or 0.38% P). Cattle performance, plasma P concentration, bone characteristics, and bone P concentration were used to determine the P requirement. Intake and ADG increased quadratically (P0.01) as dietary P increased. Plasma P in heifers receiving the 0.10% treatment was less (P0.01) than the other treatments and suggested that these heifers were experiencing a P deficiency. Total ash weight of the phalanx bones increased linearly (P0.01) as dietary P increased. In Exp. 2 using a 5 x 5 Latin square design, 5 different diets varying in P concentration (0.12, 0.27, 0.42, 0.30, and 0.36% P) were fed to steers to evaluate route and quantity of P excreted. Steers excreted little (1.78 g/d on average) P in the urine as a percentage of total P excretion. Steers on the 0.12% P diet excreted very little P in urine (0.50 g/d). Excretion of P was less (P0.05) for the cattle fed 0.12% P compared with all other treatments. Results from cattle performance, plasma P concentrations, and bone characteristics indicate that the heifers fed 0.10% P were experiencing a deficiency and the P requirement of finishing heifers is between 0.10 and 0.17% P. Dietary P concentrations of 0.10 to 0.17% P resulted in decreased P excretion. Supplementation of mineral P is unnecessary in grain-based feedlot diets because dietary P will greatly exceed the requirements (0.17%).

Three experiments were conducted to evaluate the use of combinations of wet corn gluten feed (WCGF) and wet distillers grain plus solubles (WDGS) in dry-rolled and high-moisture corn-based finishing diets for beef cattle. In Exp. 1, 250 steers (BW = 343 +/- 13.5 kg) were fed 5 treatments consisting of a corn-based, control diet with 0% coproducts, and diets including 30% WCGF, 30% WDGS, 15% WCGF plus 15% WDGS, or 30% WCGF plus 30% WDGS. No associative effects resulted from feeding 15% WCGF plus 15% WDGS; DMI, ADG, and G:F were intermediate between steers fed WCGF or WDGS at 30% of diet DM. Feeding coproducts in combinations at 30 and 60% of diet DM increased ADG, G:F, and final BW (P0.05) compared with the corn-based diet. In Exp. 2, 280 yearling steers (BW = 370 +/- 0.45 kg) were used to evaluate feeding 0, 25, 50, or 75% coproducts as a combination of 50% WCGF:50% WDGS (DM basis). Additional diets were fed containing decreased alfalfa hay at 5, 2.5, and 0% (DM basis) as coproduct blend inclusions increased at 25, 50, and 75% (DM basis), respectively. No interactions were observed between alfalfa hay and coproduct blend levels, and no effects on ADG or G:F (P0.21) were observed due to alfalfa hay. Intake, ADG, and G:F responded quadratically (P0.05) across coproduct levels, with the greatest ADG and G:F at 25 and 50% blend, and similar ADG and G:F for the 0 and 75% blend levels. In Exp. 3, 504 steers (BW = 376 +/- 16 kg) were fed to evaluate 0, 10, 15, 20, 25, and 30% (DM basis) WDGS in diets containing 30% WCGF (DM basis) as well as a control diet with no coproducts. The inclusion of 30% WCGF in the diets increased DMI, ADG, and G:F (P0.05) when compared with control. Response to inclusion level of WDGS tended to be quadratic for DMI (P = 0.12), quadratic for ADG (P = 0.05), and no effect for G:F (P = 0.96). Greatest ADG was achieved with 15 to 20% WDGS inclusion in diets containing 30% WCGF. The use of combinations of WCGF and WDGS in finishing diets resulted in similar or improved steer performance compared with corn, suggesting replacement of corn with coproduct combinations up to 75% diet DM is possible if a roughage source is fed.

In a 3-yr study, corn dried distillers grains plus solubles (DDGS) were evaluated as a substitute for forage and N fertilizer in yearling steers grazing smooth bromegrass. A total of 135 steers (330 +/- 10 kg) were used in a randomized complete block design to measure the effects of DDGS supplementation and N fertilization on animal and pasture performance. Steers were initially stocked at 6.8 animal unit month (AUM)/ha on nonfertilized smooth bromegrass pastures (CONT), at 9.9 AUM/ha on smooth bromegrass pastures fertilized with 90 kg of N/ha (FERT), or at 9.9 AUM/ha on nonfertilized smooth bromegrass pastures with 2.3 kg of DDGS DM supplemented daily (SUPP). Paddock was the experimental unit, with 3 replications per year for 3 yr. Paddocks were strip-grazed and put-and-take cattle were used to maintain similar grazing pressure among treatment paddocks during the 160-d grazing season. In vitro DM disappearance declined quadratically (P0.01), whereas CP and standing crop showed cubic responses (P0.01) throughout the grazing season. Crude protein was greater (P0.05) for FERT compared with CONT and SUPP. Standing crop was 18% greater (P0.01) for FERT than CONT and was 10% greater (P0.01) than SUPP. Adjusted stocking rates (AUM/ha) were greater (P0.01) for FERT and SUPP compared with CONT. Final BW were greater (P0.01) for SUPP steers compared with CONT and FERT steers. Similar results were observed for ADG, with SUPP steers gaining more (P0.01) compared with CONT and FERT steers. Total BW gain per hectare was increased (P0.01) by 53% with FERT and by 105% with SUPP. Feedlot ADG was similar among treatments (P = 0.88), and SUPP steers maintained their BW advantage through the finishing phase. Dried distillers grains can be used to substitute effectively for N fertilizer by increasing the performance of yearling steers grazing smooth bromegrass and increasing stocking rates compared with nonfertilized pastures.

Two experiments were conducted to determine the effect of corn processing method and corn wet distillers grains plus solubles (WDGS) level on steer performance and metabolism. In Exp. 1, 480 crossbred steer calves (314 +/- 18 kg of BW) were used in a finishing experiment with a randomized complete block design and a 3 x 4 treatment structure. Diets were based on dry-rolled (DRC), high-moisture (HMC), or steam-flaked corn (SFC) with increasing levels of WDGS (0, 15, 27.5, or 40%; DM basis). A corn processing x WDGS level interaction (P < 0.01) was observed for ADG and G:F. Average daily gain and G:F increased linearly (P < 0.01) in steers fed DRC; ADG increased quadratically (P = 0.04) and G:F increased linearly (P = 0.02) in steers fed HMC; and ADG decreased quadratically (P = 0.02) with no change in G:F (P = 0.52) in steers fed SFC as WDGS increased. In Exp. 2, 7 ruminally fistulated steers (440 +/- 41 kg of BW) were used in a 6-period crossover design with 3 x 2 factorial treatment structure. Diets were the same as those fed in Exp. 1, except they contained only 2 levels of WDGS (0 or 40% of diet DM). Total tract starch digestibility was greater (P < 0.01) for steers fed SFC than for steers fed DRC or HMC. Minimum ruminal pH was less (P < 0.01) for steers fed SFC than for steers fed HMC or DRC. Variance of ruminal pH was different among all 3 processing methods with DRC < HMC < SFC (P < 0.10). In situ 22-h DM digestibility of DRC and HMC and starch digestibility of DRC were greater (P < 0.10) in steers fed DRC compared with steers fed HMC or SFC. Steers fed 0% WDGS had less (P < or = 0.02) intake of DM, OM, NDF, and ether extract compared with steers fed 40% WDGS. Total tract digestibility of DM and OM was greater (P < or = 0.08) and digestibility of ether extract tended (P = 0.11) to be less for steers fed 0% WDGS compared with steers fed 40% WDGS. Maximum ruminal pH and pH variance were greater (P < or = 0.08) in steers fed 0% WDGS. A corn processing x WDGS level interaction (P = 0.09) was observed for ruminal acetate to propionate ratio (A:P). Within diets containing 0% WDGS, A:P in steers fed SFC was less (P < or = 0.08). In diets containing 40% WDGS, A:P was similar between processing methods and not different from the SFC with 0% WDGS. The corn processing x WDGS level interaction observed in the finishing experiment may be due to the decreased ruminal A:P in DRC and HMC diets with 40% WDGS.

A feedlot (Exp. 1) experiment was conducted to evaluate the effects of an essential oil mixture (EOM), experimental essential oil mixture (EXP), tylosin, and monensin (MON) on performance, carcass characteristics, and liver abscesses. A metabolism experiment (Exp. 2) was conducted to evaluate the effects of EOM, EXP, and MON on ruminal fermentation and digestibility in finishing steers. In Exp. 1, 468 yearling steers (398 +/- 34 kg initial BW) were used in 50 pens (10 pens/treatment) and received their respective dietary treatments for 115 d. Five dietary treatments were compared in Exp. 1: 1) control, no additives (CON); 2) EOM, 1.0 g/steer daily; 3) EXP, 1.0 g/steer daily; 4) EOM, 1.0 g/steer daily plus tylosin, 90 mg/steer daily (EOM+T); and 5) monensin, 300 mg/steer daily plus tylosin, 90 mg/steer daily (MON+T). Compared with CON, steers fed MON+T had decreased DMI (P0.01), and steers fed EOM+T and MON+T had improved G:F (P/= 0.02). Average daily gain was not different among treatments (P0.58). There was a trend (P = 0.09) for a treatment effect on 12th-rib fat thickness, which resulted in a significant increase in calculated yield grade for the EOM+T treatment. No other carcass characteristics were affected by treatment (P/= 0.10). Prevalence of total liver abscesses was reduced for steers fed tylosin compared with no tylosin (P0.05). In Exp. 2, 8 ruminally fistulated steers (399 +/- 49 kg initial BW) were assigned randomly to 1 of 4 treatments in a replicated 4 x 4 Latin square designed experiment. Treatments were 1) CON, 2) EOM, 3) EXP, and 4) MON with feeding rates similar to Exp. 1. There were no differences in DMI, OM intake, and apparent total tract DM or OM digestibilities among treatments (P0.30). Feed intake patterns were similar among feed additive treatments (P0.13). Total VFA (P = 0.10) and acetate (P = 0.06) concentrations tended to be affected by treatment with EOM numerically greater than CON. Average ruminal pH ranged from 5.59 to 5.72 and did not differ among treatments. Addition of a EOM or monensin to a diet containing tylosin improves G:F, but little difference was observed in metabolism or digestibility.

A finishing trial and a digestion trial were conducted to evaluate the effects of corn hybrid and processing method on nutrient digestibility, finishing performance, and carcass characteristics. A 2 x 5 factorial arrangement of treatments was used for both trials. Factors included 2 processing methods, dry-rolled (DRC) or high-moisture (HMC), and 5 commercially available corn hybrids. The finishing trial (Exp. 1) utilized 475 yearling steers (379 +/- 15 kg initial BW), stratified by BW into 2 blocks then assigned randomly to 1 of 60 pens (8 steers/pen). Treatments were assigned randomly to pens with 6 pens/treatment. Diets consisted of 67.5% corn (each hybrid processed as DRC or HMC), 20% wet corn gluten feed, 7.5% alfalfa hay, and 5% supplement. The digestion trial (Exp. 2) used 2 ruminally and duodenally fistulated Holstein steers (560 kg of BW) and the mobile bag technique. Bags were ruminally incubated for 22 h. For total tract digestibility, bags were subjected to a simulated abomasal pepsin digestion, inserted into the duodenum, and collected in the feces. No significant interactions between corn hybrid and processing method were observed in Exp. 1; therefore, only main effects are presented. Feeding HMC decreased (P0.01) DMI and increased (P0.01) G:F compared with cattle fed DRC. Hybrid tended to affect (P = 0.12) G:F, but did not affect (P0.36) any other variable. For Exp. 2, feeding HMC increased (P0.01) DM and starch digestibility compared with DRC, but to varying degrees depending on the hybrid. Correlating the results of the 2 trials across processing methods, strong relationships were observed between G:F and postruminal starch digestibility (r = 0.84) and total-tract starch digestibility (r = 0.73). When evaluated within processing method, these relationships weakened and were not significant. The results of these trials indicate that processing method had a larger effect on performance and digestibility than hybrid, and no interaction was observed between processing method and hybrid, suggesting hybrid effects were consistent across processing methods.

Three experiments evaluated the lipids in distillers grains plus solubles compared with corn or other sources of lipid in finishing diets. Experiment 1 utilized 60 individually fed yearling heifers (349 +/- 34 kg of BW) fed treatments consisting of 0, 20, or 40% (DM basis) wet distillers grains plus solubles (WDGS), or 0, 2.5, or 5.0% (DM basis) corn oil in a finishing diet based on high-moisture corn (HMC) and dry-rolled corn. Cattle fed 20 and 40% WDGS had greater (P0.10) G:F than cattle fed 0% WDGS. Cattle fed the 5.0% corn oil had less overall performance than cattle fed the other diets. Results from Exp. 1 indicated that adding fat from WDGS improves performance, whereas supplementing 5.0% corn oil depressed G:F, suggesting that the fat within WDGS is different than corn oil. Experiment 2 used 234 yearling steers (352 +/- 16 kg of BW) fed 1 of 5 treatments consisting of 20 or 40% (DM basis) dry distillers grains plus solubles, 1.3 or 2.6% (DM basis) tallow, or HMC. All diets contained 20% (DM basis) wet corn gluten feed as a method of controlling acidosis. No differences between treatments for any performance variables were observed in Exp. 2. The dry distillers grains plus solubles may be similar to tallow and HMC in finishing diets containing 20% wet corn gluten feed. Experiment 3 used 5 Holstein steers equipped with ruminal and duodenal cannulas in a 5 x 5 Latin square design. Treatments were a 40% WDGS diet, 2 composites, one consisting of corn bran and corn gluten meal; and one consisting of corn bran, corn gluten meal, and corn oil; and 2 dry-rolled corn-based diets supplemented with corn oil or not. Cattle fed the WDGS diet had numerically less rumen pH compared with cattle fed other treatments. Cattle fed WDGS had greater (P0.10) molar proportions of propionate, decreased (P0.10) acetate:propionate ratios, greater (P0.10) total tract fat digestion, and a greater (P0.10) proportion of unsaturated fatty acids reaching the duodenum than cattle fed other treatments. Therefore, the greater energy value of WDGS compared with corn may be due to more propionate production, greater fat digestibility, and more unsaturated fatty acids reaching the duodenum.

Crossbred heifers (n = 120; 265 kg, SD = 37) were fed individually (84 d) to determine the effect of supplement type, concentration, and frequency on intake and performance and to estimate the energy value of dry distillers grains plus solubles (DDGS) in a high-forage diet. Treatments were arranged in a 3 x 2 x 2 factorial, with 3 supplements, 2 concentrations, and 2 frequencies of supplementation. Supplements including dry-rolled corn (DRC), DRC with corn gluten meal (DRC + CGM), and DDGS were fed at 0.21% (LOW) or 0.81% (HIGH) of BW daily and were provided daily (DAILY) or 3 times weekly (ALT). Heifers were fed to consume grass hay (8.7% CP) ad libitum. Individual DMI, diet composition, BW, and ADG were used to calculate energy values for DDGS and DRC. Supplement type, concentration, frequency, and interactions were tested using the MIXED procedure of SAS, with BW included as a covariate. Supplement x concentration interactions for gain (P = 0.01) and G:F (P0.01) were detected. At the LOW concentration, heifers supplemented with DDGS gained more and were more efficient (P/= 0.03) than those supplemented with DRC or DRC + CGM. No performance differences were observed (P/= 0.22) between DDGS and DRC + CGM in HIGH treatments, although both improved (P/= 0.01) gain and G:F relative to DRC. Calculated TDN content of DDGS was 18 to 30% greater than DRC. Gain and G:F were improved (P0.01) in heifers fed HIGH vs. LOW. Total intake was greater (P0.01) for HIGH than LOW, but LOW heifers consumed more hay (P0.01) than HIGH. The DAILY heifers consumed more (P0.01) hay and total DM than the ALT heifers. The DAILY heifers gained more (P0.01) than ALT, but G:F was not affected (P = 0.85) by supplementation frequency. In a high-forage diet, DDGS has greater energy value than corn.

Beef knuckles (n = 160) were obtained from source-verified cattle finished on 30% wet distillers grains plus solubles enriched with varying levels of alfalfa hay (4 or 8%), corn silage (6 or 12%), or corn stalks (3 or 6%) based on NDF. Proximate analysis, pH, oxidation-reduction potential, fatty acid composition, and sensory analysis were conducted on the rectus femoris muscle to determine if roughage inclusion, in conjunction with wet distillers grains plus solubles and cattle source, affects beef flavor with particular interest in liver-like off-flavor. Proximate analysis, fat content, and oxidation-reduction potential were unaffected (P ge;0.129) by diet or source. For s.c. adipose tissue, cattle from Nebraska (NE) had greater amounts of MUFA (P = 0.048) and unsaturated fatty acids (P = 0.068) but less SFA (P = 0.065) when compared with cattle from South Dakota. Diet affected s.c. adipose tissue levels of 15:0, 17:0, and n-3 fatty acids in which cattle from NE finished on the low corn stalk diet had (Por =0.050) lower levels. Cattle from NE had (Por = 0.049) greater i.m. adipose proportions of 13:0 and CLA. Dietary effects (Por = 0.050) were observed for i.m. adipose tissue proportions of 16:0, 18:1(n-9), 18:2(n-6), 20:4(n-6), 22:5(n-3), MUFA, PUFA, and n-6 fatty acids. Sensory analysis revealed that cattle from NE were (Por = 0.023) less juicy and had less bloody notes when compared with cattle from South Dakota. Cattle finished on the low alfalfa diet were (Por = 0.014) more tender and juicy but had more bloody notes. No (P ge; 0.670) dietary or source effects were noted for liver-like off-flavor. Subcutaneous amounts of 18:2(n-6 trans) (r = -0.17) were inversely related to the incidence of liver-like off-flavor, whereas 20:1(n-9) (r = 0.21), CLA cis-9, trans-11 (r = 0.16) were directly related. Data from this study indicate that type and level of roughage inclusion and cattle source have minimal effects on fatty acid profiles and sensory properties of the musculus rectus femoris. However, individual fatty acids of s.c. and i.m. adipose tissue were significantly correlated with liver-like off-flavor.

The ethanol industry is expanding rapidly. This expansion in production of renewable energy also increases production of by-products. These byproducts, primarily distillers grains plus solubles (DGS), are utilized very efficiently by ruminants. When the starch in corn is fermented to produce ethanol, the remaining nutrients (protein, fat, fiber) are concentrated about 3-fold. Whereas DGS is an excellent protein source for ruminants, the large supply and the price relative to corn make DGS an attractive energy source as well. This is especially important with reduced availability and higher price of corn because of demand by the ethanol industry. A meta-analysis of 9 experiments, where various levels of wet DGS were fed to feedlot cattle, shows that wet DGS produced higher ADG and G:F compared with cattle fed corn-based diets without DGS. A similar analysis with dry DGS showed similar type of responses but with less apparent feeding value for dry DGS compared with wet DGS. Metabolism studies suggest the fat in DGS may be partially protected from ruminal degradation leading to greater proportion of unsaturated fatty acids at the duodenum and greater total tract fat digestibility. Both the fat and the undegradable protein in DGS appear to explain some but not all of the greater feeding value of DGS compared with corn. Lower quality roughages may be used in feedlot diets containing wet DGS because of the protein, moisture, and physical characteristics the DGS contains. The feeding value of DGS is greater than dry-rolled corn or high moisture corn; however, the feeding value of DGS appears to be less when fed in finishing diets based on steam-flaked corn than in those based on dry-rolled or high-moisture corn.

Two experiments evaluated prebreeding target BW or progestin exposure for heifers developed lighter than traditional recommendations. Experiment 1 evaluated the effects of the system on heifer performance through subsequent calving and rebreeding over 3 yr. Heifers (229 kg) were assigned randomly to be developed to 55% of mature BW (299 kg) before a 45-d breeding season (intensive, INT; n = 119) or 50% of mature BW (272 kg) before a 60-d breeding season (relaxed, RLX; n = 142). Prebreeding and pregnancy diagnosis BW were greater (Por= 0.006) for INT than RLX heifers. Overall pregnancy rate did not differ (88.4%; P = 0.51), but RLX heifers had later calving dates (7 d; P0.001) and lighter calf weaning weights (194 +/- 4 vs. 199 +/- 4 kg; P0.07) compared with INT heifers. Calf birth weight, calving difficulty, second-calf conception rates, and 2-yr-old retention rate did not differ (P0.15) between systems. Cost per pregnant 2-yr-old cow was less for the RLX than the INT heifer development system. Of heifers that failed to become pregnant, a greater proportion (P = 0.07) of heifers in the RLX than in the INT system were prepubertal when the breeding season began. Therefore, a second 2-yr experiment evaluated melengestrol acetate (MGA, 0.5 mg/d) as a means of hastening puberty in heifers developed to 50% of mature BW. Heifers were assigned randomly to the control (n = 103) or MGA (n = 81) treatment for 14 d and were placed with bulls 13 d later for 45 d. Prebreeding and pregnancy diagnosis BW were similar (280 and 380 kg, respectively; P0.10) for heifers in the control and MGA treatments. The proportion of heifers pubertal before breeding (74%), pregnancy rate (90%), calving date, calf weaning weight, and second breeding season pregnancy rate (92%) were similar (P0.10) between treatments. Developing heifers to 50 or 55% of mature BW resulted in similar overall pregnancy rates, and supplementing the diets of heifers developed to 50% of mature BW with MGA before breeding did not improve reproductive performance.

Crossbred heifers (n = 120; BW = 368 kg, SD = 39 kg) were used to determine effects of dried distillers grains (DDG) and relative contributions of undegradable intake protein (UIP) and fat (ether extract, EE) in DDG on ADG and forage intake (FI). Heifers rotationally grazed six 3.5-ha, smooth bromegrass paddocks (IVDMD = 65.7%, CP = 20.8%, UIP = 2.17%, DM basis). Heifers were blocked by previous ADG and allotted to treatments in a 3 x 3 + 1 factorial design. Factors were source and level of supplementation. Supplements were as follows: 1) DDG (UIP = 15.8%, EE = 9.67%), 2) corn gluten meal (CGM; UIP = 31.6%, EE = 0.83%), or 3) corn oil (OIL; UIP = 0.74%, EE = 19.3%). Amounts of DDG were 750, 1,500, or 2,250 g/d, whereas amounts of CGM and OIL were 375, 750, or 1,125 g/ d. Supplements containing CGM and OIL were fed in amounts that provided UIP and EE, respectively, equivalent to those of the DDG. Contrasts of interest were DDG vs. CGM and DDG vs. OIL. Control heifers were fed 250 g/d of a supplement containing corn bran and molasses (UIP = 0.92%, EE = 1.13%). Heifers were supplemented individually. Treatments were separated by regressing the response variables on grams of nutrient (DM, UIP, or EE) intake per kilogram of BW, because not all heifers consumed their allotment of supplement. Supplemental DDG resulted in a linear increase in ADG (P0.01), whereas CGM tended to increase ADG (P = 0.14) but at a rate that was 39% of that for DDG, representing a response to MP. Supplementation of OIL did not affect ADG (P = 0.25) and tended to result in ADG less than that of DDG (P = 0.09). Supplementation with DDG had no effect (P = 0.63) on FI when predicted by the use of chromic oxide but tended (P = 0.07) to decrease FI when it was predicted from ADG using NE equations. Despite the differences between methods in the significance of the effect of DDG, the rates of substitution agreed (-0.50 and -0.45 for chromic oxide and NE equations, respectively), suggesting that the chromic oxide method was less sensitive in assessing FI. Supplementation with CGM decreased FI (P0.01), but FI for CGM did not differ from that of DDG when the chromic oxide method was used (P = 0.19). Corn oil had no effect on FI (P = 0.42). Increased ADG and decreased FI observed from DDG supplementation is not independently explained by UIP or EE contained in DDG.

Ten ruminally cannulated heifers (BW = 416 kg; SD = 24) were used to test the effect of the form and frequency of supplemental energy on forage DMI and digestibility. Five treatments were arranged in a replicated, 5 x 4 Latin rectangle (n = 8), and included no supplement (control), dry-rolled corn (DRC) fed daily, DRC fed on alternate days (DRC-A), dried distillers grains plus solubles (DDGS) fed daily, and DDGS fed on alternate days (DDGS-A). Supplements fed daily were fed at 0.40% of BW, whereas alternate day-fed supplements were fed at 0.80% of BW every other day. Chopped grass hay (8.2% CP) was fed to allow ad libitum DMI, and the intake pattern was measured. Control heifers had greater (P0.01) hay DMI than supplemented heifers (1.88 vs. 1.66% of BW daily, respectively), although total DMI was lower (P0.01) for control. Hay DMI did not differ (P = 0.45) between DRC and DDGS, and tended to be lower (P = 0.08) by heifers on DDGS-A and DRC-A than by heifers supplemented daily. Hay intake was lower (P0.01) on supplementation days for DDGS-A and DRC-A than on nonsupplemented days. Heifers in alternate-day treatments had fewer (P0.01) and larger (P0.01) meals and spent less (P0.01) time eating than those supplemented daily. Average rumen pH was greater (P = 0.05) for control than supplemented heifers (6.30 vs. 6.19). Control heifers had greater (P = 0.04) rates and extents of NDF disappearance than supplemented heifers. Rate of hay NDF disappearance was lower (P = 0.02) for DRC than for DDGS. Supplementation decreased hay DMI and changed digestion kinetics. Supplementation frequency affected amount and pattern of DMI. Rate of hay NDF disappearance was greater for DDGS than DRC.

Two experiments were conducted to determine the influence of chemical and physical corn kernel traits on digestibility and feedlot cattle performance. Seven commercially available corn hybrids representing a range in kernel traits were evaluated for a variety of chemical and physical traits that included test weight, 1,000-grain weight, kernel size, starch, CP, amylose, Stenvert Hardness tests (kernel hardness traits), tangential abrasive dehulling device loss, 12-h in vitro starch disappearance, and rate and extent of in situ DM disappearance. Differences among hybrids existed for all physical kernel traits measured. In Exp. 1, 224 steers in 28 pens were fed the same hybrids for 167 d in a completely randomized design. All diets were formulated to have 12.5% CP and contained 66% dry-rolled corn (DM basis). There were no differences (P0.20) among corn hybrids for DMI, ADG, or carcass characteristics. However, efficiency of gain (G:F) was influenced by hybrid (P0.01) with a difference of 9.5% from the least to the most efficient. In Exp. 2, 7 ruminally cannulated heifers were used in a 7 x 7 Latin square design to determine the effects of these hybrids on nutrient digestibility, VFA concentrations, and ruminal pH. Total-tract OM and starch digestibilities were not different (P0.15) among hybrids and averaged 77.9 and 95.1%, respectively. Differences (P0.05) among hybrids existed for ruminal propionate concentration and the acetate to propionate ratio. Kernel hardness traits correlated (P0.05) with G:F were 1,000-grain weight (r = -0.81), Stenvert time to grind (r = -0.83), and the proportion of Stenvert soft to coarse particle height (r = 0.83). Propionate concentration was not correlated (r = 0.45) with G:F but was correlated (P = 0.02) to the Stenvert time to grind (r = -0.83). Cattle fed dry-rolled corn hybrids with greater proportions of soft endosperm had greater concentrations of propionate and gained more efficiently than cattle fed hybrids with a harder endosperm. Selecting for these softer kernel traits may improve the efficiency of gain in feedlot cattle.

One-hundred ninety-two crossbred steers (initial BW = 351 +/- 11 kg) were used to determine the effects of removing alfalfa hay (AH) from dry-rolled corn-based diets containing wet corn gluten feed (WCGF) on animal performance and nutrient (N and OM) mass balance in open feedlot pens. Steers were stratified by weight and assigned randomly to 24 pens (2 x 3 factorial) and fed for 132 d from June to October 2002. Experimental diets contained either 0 or 35% WCGF and 0, 3.75, or 7.5% AH, and were formulated to be isonitrogenous. For efficiency of gain, an interaction occurred (P = 0.09) between AH and WCGF. Feed efficiencies of cattle fed 35% WCGF were improved 4.4% (P = 0.10) compared with efficiencies of cattle fed no WCGF at 0% AH; there was a marked improvement in ADG for cattle fed WCGF compared with no WCGF in diets with 0% AH. Within 35% WCGF diets, efficiency decreased as AH inclusion increased (P = 0.06). Efficiency was equal across AH levels when 0% WCGF was fed; however, ADG was decreased when AH was removed. Interactions between AH and WCGF were not detected for other performance or carcass criteria; therefore, main effects of AH and WCGF are discussed. Daily intake, ADG, and HCW increased linearly (P0.05) as dietary AH level increased. Feeding 35% WCGF also resulted in greater DMI (P0.01) and a tendency for greater ADG and HCW (Por = 0.10) compared with steers fed no WCGF. Interactions between AH and WCGF were not observed for feedlot N mass balance. As level of AH increased across diets, N intake, N retention, and N excretion increased (P0.05). Steers fed 35% WCGF consumed and excreted more N (P0.01) than those fed no WCGF. More manure DM (P = 0.11), OM, and N (P0.01) were removed from pens housing steers fed 35% WCGF as well as greater OM and N recovery in finished compost. More N (kilogram/steer) was also lost to volatilization as a result of greater N excretion when WCGF was fed. Expressed as a percentage of N excretion, loss of N from pens housing steers fed 0 and 35% WCGF was not different, averaging nearly 80%. These data suggest that AH has less value when dry-rolled corn-based diets contain 35% WCGF and can be decreased from conventional levels. Furthermore, loss of N from open feedlot pens is high during the summer months, and feeding WCGF may not reduce N losses during these times of year.

Two experiments were conducted using 2 ruminally and duodenally fistulated steers to determine the digestibility of undegradable intake protein (UIP) of smooth bromegrass (Bromis inermis), birdsfoot trefoil (Lotus coniculatus L.), and heat-treated alfalfa (Medicago sativa) using the mobile nylon bag technique. Undegradable intake protein was determined using neutral detergent insoluble CP at a single in situ incubation time point based on 75% of the total mean retention time estimated from IVDMD plus a 10-h passage lag. In Exp. 1, UIP (% DM) of smooth bromegrass in June and July were 1.82 and 1.71, respectively (P = 0.11). Undegradable intake protein (% DM) of birdsfoot trefoil increased from 1.30 in June to 1.94 in July (P0.01). Total tract indigestible protein of smooth brome-grass and birdsfoot trefoil increased in July (P0.05). Digestibility of UIP decreased in July for smooth brome-grass (P0.01) but tended to increase for birdsfoot trefoil (P = 0.07). In Exp. 2, alfalfa from plots fertilized with low (66 kg of N/ha) or high (200 kg of N/ha) amounts of N were dried to simulate 3 preservation methods: dehydrated (100 degrees C, 10 h), sun-cured (50 degrees C, 15 h), and lyophilized (-50 degrees C, 72 h) alfalfa. Undegradable intake protein (% DM) was estimated as in Exp. 1 and was 3.13, 2.10, and 1.84 for dehydrated, sun-cured, and lyophilized alfalfa, respectively. Total tract indigestible protein (% DM) was increased (P0.05) for dehydrated alfalfa (1.66) compared with sun-cured (1.54) or lyophilized (1.57) alfalfa. As a result of greater UIP flow to the lower tract, digestibility (%) of UIP was greater (P0.01) for dehydrated (46.4) than for sun-cured (25.6) or lyophilized (14.7) alfalfa. Heat-treated alfalfa samples increased net UIP absorption in the lower tract because 1.47, 0.56, and 0.27 percentage units of UIP (% DM) of dehydrated, sun-cured, and lyophilized alfalfa, respectively, disappeared. Overall, the digestibility of the UIP of these forages was low in the lower tract.

Two data sets were developed to evaluate and refine feed energy predictions with the beef National Research Council (NRC, 1996) model level 1. The first data set included pen means of group-fed cattle from 31 growing trials (201 observations) and 17 finishing trials (154 observations) representing over 7,700 animals fed outside in dirt lots. The second data set consisted of 15 studies with individually fed cattle (916 observations) fed in a barn. In each data set, actual ADG was compared with ADG predicted with the NRC model level 1, assuming thermoneutral environmental conditions. Next, the observed ADG (kg), TDN intake (kg/d), and TDN concentration (kg/kg of DM) were used to develop equations to adjust the level 1 predicted diet NEm and NEg (diet NE adjusters) to be applied to more accurately predict ADG. In both data sets, the NRC (1996) model level 1 inaccurately predicted ADG (P0.001 for slope = 1; intercept = 0 when observed ADG was regressed on predicted ADG). The following nonlinear relationships to adjust NE based on observed ADG, TDN intake, and TDN concentration were all significant (P0.001): NE adjuster = 0.7011 x 10(-0.8562 x ADG) + 0.8042, R2 = 0.325, s(y.x) = 0.136 kg; NE adjuster = 4.795 10(-0.3689 x TDN intake) + 0.8233, R2 x = 0.714, s(y.x) = 0.157 kg; and NE adjuster = 357 x 10(-5.449 x TDN concentration) + 0.8138, R2 = 0.754, s(y.x) = 0.127 kg. An NE adjuster1 indicates overprediction of ADG. The average NE adjustment required for the pen-fed finishing trials was 0.820, whereas the (P0.001) adjustment of 0.906 for individually fed cattle indicates that the pen-fed environment increased NE requirements. The use of these equations should improve ADG prediction by the NRC (1996) model level 1, although the equations reflect limitations of the data from which they were developed and are appropriate only over the range of the developmental data set. There is a need for independent evaluation of the ability of the equations to improve ADG prediction by the NRC (1996) model level 1.